[Effect of xy2004, a centchroman derivative, on proliferation of MCF-7 cells in vitro and the mechanism].

Nan Fang Yi Ke Da Xue Xue Bao

Department of Pharmacology, Xi'an Medical College, Xi'an 710068, China.E-mail:

Published: October 2014

AI Article Synopsis

  • The study aimed to understand how xy2004, a derivative of centchroman, affects the growth of MCF-7 breast cancer cells and the mechanisms behind it.
  • Results showed that at low concentrations, xy2004 promotes cell growth, while high concentrations lead to reduced growth; this effect is influenced by tamoxifen and changes in apoptosis-related proteins.
  • The findings indicate that xy2004 interacts with estrogen receptors and alters the expression of crucial proteins like Bcl-2 and Bax, highlighting its dual role in promoting or inhibiting cell proliferation based on concentration.

Article Abstract

Objective: To investigate the effect of xy2004, a centchroman derivative, on the proliferation of MCF-7 cells and the mechanisms.

Methods: The effects of xy2004 on MCF-7 cell proliferation and apoptosis were evaluated with MTT assay and flow cytometry, respectively. The expressions of the apoptosis-related proteins were examined with Western blotting. Competitive estrogen-receptor binding assay was used to investigate the affinity of xy2004 to estrogen receptors (ER).

Results: xy2004 induced proliferation of MCF-7 cells at low concentrations but inhibited cell proliferation at high concentrations. The application of tamoxifen inhibited xy2004-induced proliferation of MCF-7 cells. The relative binding affinity of xy9906 to ERα and ERβ, presented as the IC50 value, was 7.38 × 10⁻³ mol/L and 4.12 × 10⁻⁷ mol/L, respectively. Treatment of MCF-7 cells with high-concentration xy2004 reduced the cellular expression of Bcl-2 protein and increased Bax protein expression.

Conclusion: At low concentrations, xy2004 directly stimulates the proliferation of MCF -7 cells through ligand-receptor binding, and at high concentrations, it inhibits the cell proliferation by regulating the expression levels of the apoptosis-related proteins.

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